Immunotherapy for Urothelial Carcinoma: Current Evidence and Future Directions

被引:42
|
作者
Tripathi, Abhishek [1 ]
Plimack, Elizabeth R. [2 ]
机构
[1] Univ Oklahoma, Stephenson Canc Ctr, Hematol Oncol, 800 NE 10th St,6th Floor, Oklahoma City, OK USA
[2] Fox Chase Canc Ctr, Dept Hematol Oncol, Div Genitourinary Med Oncol, 333 Cottman Ave, Philadelphia, PA 19111 USA
关键词
Bladder cancer; Urothelial carcinoma; Immunotherapy; PD-1; Checkpoint inhibitors; CISPLATIN-INELIGIBLE PATIENTS; CYTOTOXIC T-LYMPHOCYTES; BLADDER-CANCER; SINGLE-ARM; CALMETTE-GUERIN; OPEN-LABEL; PHASE-II; MULTICENTER; CHEMOTHERAPY; PD-1;
D O I
10.1007/s11934-018-0851-7
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of ReviewUntil recently, effective treatment options for patients with advanced urothelial carcinoma were limited to platinum-based chemotherapy. In the post-platinum setting and for patients ineligible for cisplatin, minimally effective second-line chemotherapy was used and outcomes were poor. The approval of immune checkpoint inhibitors has significantly changed the treatment landscape of urothelial carcinoma. Here, we review current data demonstrating their efficacy in advanced disease and ongoing trials investigating novel combination strategies.Recent FindingsSince May 2016, five agents targeting the programmed cell death 1 (PD-1) pathways have been approved for use after progression on platinum-based chemotherapy. Further, atezolizumab and pembrolizumab are approved for use in cisplatin-ineligible patients with high programmed death-ligand 1 (PD-L1) expression. Preliminary studies have shown their safety and efficacy as neoadjuvant therapy in muscle-invasive bladder cancer. Several ongoing trials are investigating these agents in combination with radiation therapy, platinum-based chemotherapy, other immune checkpoint inhibitors, and targeted agents.SummaryImmune checkpoint inhibitors have demonstrated durable efficacy in patients with advanced urothelial carcinoma as first- and second-line therapy. Ongoing studies will help define the optimal sequence, combination strategies, and predictive biomarkers of response.
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页数:10
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